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EMA Product

Rasagiline ratiopharm

Product approved by European Medicines Agency (EU)

Basic Information

Rasagiline ratiopharm

Regulatory Information

EMEA/H/C/003957

Authorised

January 12, 2015

November 20, 2014

10

April 9, 2025

Company Information

Netherlands

Swensweg 5 2031 GA Haarlem

Teva Pharma B.V.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Rasagiline ratiopharm is indicated for the treatment of idiopathic Parkinson’s disease (PD) as monotherapy (without levodopa) or as adjunct therapy (with levodopa) in patients with end of dose fluctuations.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Rasagiline ratiopharm. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Rasagiline ratiopharm. For practical information about using Rasagiline ratiopharm, patients should read the package leaflet or contact their doctor or pharmacist.

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